Job Description

Kenvue is currently recruiting for a:

Associate MA Manager

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here

Role reports to:

资深医学事务经理

Location:

Asia Pacific, China, Shanghai, Shanghai

Work Location:

Hybrid

What you will do

Administers medical affairs programs management, safety reporting, data coordination/management and reporting/communication of results ( for example, publication, presentations, communication materials). Participates in developing policies and procedures for development and provision of medical an. Research educational and technical materials in support of local and regional speakers upon unsolicited request. Organizes technical information and education regarding the safe and effective use of company products to health care providers and other customers. Plans clinical educational activities that facilitate learning regarding clinically relevant information to physicians, nurses, and other medical professionals. Screening and processing of unsolicited medical education grants for therapeutic and operational appropriateness. Supports medical operations. Participates in the company's drug surveillance program which includes following up on adverse reaction reports. Provides solutions surrounding legal liability and compliance with government regulations. Oversees quantitative and qualitative data analysis. Facilitates understanding of clinical trial data. Ensures the quality and integrity of the data generated from clinical trials. Maintains relationships with internal stakeholders to ensure the information integrity. Integrates appropriate information into training programs.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.